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Ecology and Evolution
Article . 2019 . Peer-reviewed
License: CC BY
Data sources: Crossref
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Ecology and Evolution
Article
License: CC BY
Data sources: UnpayWall
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PubMed Central
Article . 2019
Data sources: PubMed Central
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Genome streamlining via complete loss of introns has occurred multiple times in lichenized fungal mitochondria

Authors: Cloe S. Pogoda; Kyle G. Keepers; Arif Y. Nadiadi; Dustin W. Bailey; James C. Lendemer; Erin A. Tripp; Nolan C. Kane;

Genome streamlining via complete loss of introns has occurred multiple times in lichenized fungal mitochondria

Abstract

AbstractReductions in genome size and complexity are a hallmark of obligate symbioses. The mitochondrial genome displays clear examples of these reductions, with the ancestral alpha‐proteobacterial genome size and gene number having been reduced by orders of magnitude in most descendent modern mitochondrial genomes. Here, we examine patterns of mitochondrial evolution specifically looking at intron size, number, and position across 58 species from 21 genera of lichenized Ascomycete fungi, representing a broad range of fungal diversity and niches. Our results show that thecox1gene always contained the highest number of introns out of all the mitochondrial protein‐coding genes, that high intron sequence similarity (>90%) can be maintained between different genera, and that lichens have undergone at least two instances of complete, genome‐wide intron loss consistent with evidence for genome streamlining via loss of parasitic, noncoding DNA, inPhlyctis boliviensisandGraphis lineola. Notably, however, lichenized fungi have not only undergone intron loss but in some instances have expanded considerably in size due to intron proliferation (e.g.,Alectoria fallacinaandParmotrema neotropicum), even between closely related sister species (e.g.,Cladonia). These results shed light on the highly dynamic mitochondrial evolution that is occurring in lichens and suggest that these obligate symbiotic organisms are in some cases undergoing recent, broad‐scale genome streamlining via loss of protein‐coding genes as well as noncoding, parasitic DNA elements.

Country
United States
Keywords

parasitic genetic elements, introns, genome reduction, homing endonucleases, lichen, symbiosis, Original Research

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
32
Top 10%
Top 10%
Top 10%
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